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- source_evidence_literature type ECO_0000212 NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion description "[The patient is heterozygous for an alteration in the A2M gene; this may be responsible for his serum A2M deficiency and may be relevant to the early onset of pulmonary disease in his case.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion evidence source_evidence_literature NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion SIO_000772 2475424 NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion wasDerivedFrom befree-2016 NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_assertion wasGeneratedBy ECO_0000203 NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1175607.RAsnjrbXvOx-nIHb3rkbPrEFT7tSk1lOtX3jh554eev2U130_provenance.